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Organopolysilozane compositions crosslinkable with elimination of alcohols to give elastomer

a technology of organic polysilozane and composition, which is applied in the field of alkoxy rtv1 composition, can solve the problems of compromising the consistency of the rtv-1 system, unsatisfactory stress-strain behavior of compositions used as permanently flexible sealing materials, and marked increase the danger of adhesion failure. , to achieve the effect of low modulus and convenient us

Inactive Publication Date: 2001-07-03
WACKER CHEM GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

An object of the invention is to provide a simple way of manufacturing alkoxy RTV-1 compositions which are easy to use and which, without adding plasticizer, can be adjusted to have a low modulus. For the purposes of the present invention, the term organopolysiloxanes is intended to include dimeric, oligomeric and polymeric siloxanes.
Another advantage of this process is that no side-reactions occur and, for example, no formation of T units or Q units is observed on linear HO-terminated organopolysiloxanes (A). The acid phosphoric esters (C) do not have to be deactivated immediately after the reaction.

Problems solved by technology

Unplasticized RTV-1 (room temperature vulcanizable, one part) compositions have unsatisfactory stress-strain behavior for use as permanently flexible sealing materials, since the stress values at, for example, 100% strain ("modulus at 100% strain") are too high.
A high 100% modulus (e.g. 0.6 N / mm.sup.2) is associated with a marked increase in stress in the event of widening of the joint, caused for example by changes in temperature, which markedly increases the danger of adhesion failure, i.e. detachment of the flexible sealing material from the respective joint substrate.
However, the use of very long-chain polymers compromises the consistency of the RTV-1 system.
Thus, if the consistency of the filled paste is to be soft and paste-like but also self-supporting, the viscosity of the organopolysiloxane cannot be too high, otherwise the result is a stiff, putty-like paste which is difficult to use.
The fundamental disadvantage of a plasticizer is that it is not chemically bound to the vulcanizate network.
This phenomenon becomes particularly noticeable with joints in porous natural stone, such as marble, granite or altoquartzite, since the periphery of the joint becomes hydrophobicized and darkens therefore permanently, and this is of course undesirable.
However, this process requires an excessive number of operations and gives unvulcanized compositions which are undesirably stiff.
The disadvantages of such preparation need not be stated.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1 (

inventive)

850 g of a dimethylpolysiloxane which has a hydroxyl group in each terminal unit and has a viscosity of 20,000 mPa.multidot.s at 23.degree. C. are mixed, in a planetary mixer which can operate under vacuum, with 12 g of a mixture of alkoxylated phosphoric esters of the formulae

(OH).sub.1 PO[(OCH.sub.2 CH.sub.2).sub.2-3 --O--(CH.sub.2).sub.7-9 --CH.sub.3 ].sub.2 and

(OH).sub.2 PO[(OCH.sub.2 CH.sub.2).sub.2-3 --O--(CH.sub.2).sub.7-9 --CH.sub.3 ].sub.1.

20 g of methyltrimethoxysilane, 10 g of vinyltrimethoxysilane and 10 g of dimethyldimethoxysilane are then immediately added, followed by homogenization at room temperature under normal pressure for 10 minutes. The following are then added in the sequence given, using the mixing techniques usual for RTV-1 compositions:

85 g of pyrogenic, hydrophilic silica with a BET surface area of 150 m.sup.2 / g, 18 g of amino-functional siloxane which is the equilibration product made from aminopropyltriethoxysilane and a condensate / hydrolysat...

example 2 (

inventive)

The procedure is similar to that of Example 1. 850 g of the .alpha.,.omega.-dihydroxypolydimethylsiloxane of Example 1 are mixed with 15 g of a mixture of alkoxylated phosphoric esters of the formulae

(OH).sub.1 PO[(OCH.sub.2 CH.sub.2).sub.3-4 --O--(CH.sub.2).sub.11-14--CH.sub.3 ].sub.2 and

(OH).sub.2 PO[(OCH.sub.2 CH.sub.2).sub.3-4 --O--(CH.sub.2).sub.11-14--CH.sub.3 ].sub.1.

To this the following ingredients are added in the sequence given:

22 g of methyltrimethoxysilane, 11 g of vinyltrimethoxysilane, 17 g of dimethyldimethoxysilane, 18 g of amino-functional siloxane which is the equilibration product made from aminopropyltriethoxysilane and a condensate / hydrolysate of methyltriethoxysilane with an amine number of 2.2, 4 g of 3-(2-aminoethylamino)propyltriethoxysilane, 85 g of pyrogenic, hydrophilic silica with a BET surface area of 150 m.sup.2 / g, and 4 g of the reaction product of tetraethyl silicate and di-n-butyltin diacetate from Example 1.

The skin-formation time of th...

example 3

The procedure is similar to that of Example 1. The following ingredients are admixed in the sequence given, employing 850 g of the .alpha.,.omega.-dihydroxypolydimethylsiloxane of Example 1: 15 g of the alkoxylated phosphoric ester of Example 2, 17 g of methyltrimethoxysilane, 8 g of vinyltrimethoxysilane and 25 g of dimethyldimethoxysilane are then added immediately, followed by homogenization in vacuo for 10 minutes. The following are then added in the sequence given, using the mixing techniques usual for RTV-1 compositions: 18 g of amino-functional siloxane which is the equilibration product made from aminopropyltriethoxysilane and a condensate / hydrolysate of methyltriethoxysilane with an amine number of 2.2, 4 g of 3-(2-aminoethylamino)propyltriethoxysilane, 85 g of pyrogenic, hydrophilic silica with a BET surface area of 150 m.sup.2 / g, and 4 g of the reaction product of tetraethyl silicate and di-n-butyltin diacetate from Example 1.

The skin-formation time of the composition du...

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Abstract

Alkoxy RTV-1 compositions comprise the product of the reaction of(A) an HO-terminated organopolysiloxane,(B1) an alkoxysilane which has at least three alkoxy groups and / or its partial hydrolysates, and(B2) an alkoxysilane which has two alkoxy groups and / or its partial hydrolysates, in the presence of(C) an acid phosphoric ester of the general formula (I)wherea is 1 or 2,R1 and R2 are a hydrogen radical, methyl radical or hydroxyl radical,b and d are 2 or 3,c is an integer from 2 to 15,e is 0 or 1L comprises a radical -O-, -COO-, -OOC-, -CONR3-, -NR4CO- or -CO-,R3 and R4 are a hydrogen radical or C1-C10-alkyl radical, andM is a monovalent, unsubstituted or hydroxyl-, fluorine-, chlorine-, bromine-,C1-C10-alkoxyalkyl- or cyano-substituted C1-C20-hydrocarbon radical, with the proviso that on any given carbon atom not more than one radical R1 and R2 may be a hydroxyl radical.

Description

The invention relates to alkoxy RTV-1 compositions which give low-modulus vulcanizates, to the preparation of these compositions, and to their use as sealing compounds for filling joints in natural stone.Unplasticized RTV-1 (room temperature vulcanizable, one part) compositions have unsatisfactory stress-strain behavior for use as permanently flexible sealing materials, since the stress values at, for example, 100% strain ("modulus at 100% strain") are too high. A high 100% modulus (e.g. 0.6 N / mm.sup.2) is associated with a marked increase in stress in the event of widening of the joint, caused for example by changes in temperature, which markedly increases the danger of adhesion failure, i.e. detachment of the flexible sealing material from the respective joint substrate. It has been found in practice, that a 100% modulus of from 0.2 to 0.4 N / mm.sup.2 is desirable for this type of joint.The stress-strain behavior of a silicone rubber vulcanizate is a function of the type and amount...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): C08K5/00C08K5/521C08L83/00C08L83/04C08G77/38C08K5/5419C08L71/00C08L83/06
CPCC08K5/521C08L83/04C08G77/14C08G77/16C08G77/18C08G77/24C08G77/26C08L83/00C08L2666/28
Inventor FINGER, CHRISTIANDORSCH, NORMANHECHTL, WOLFGANGBAUMGARTNER, CHRISTIANHEINRICH, ALFRED
Owner WACKER CHEM GMBH
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